Home GUDID 26950900932490 INT,SlideCath
Primary DI 26950900932490
Brand INT,SlideCath
Company Shanghai Kindly Medical Instruments Co., Ltd.
Model ACJR404F1100
Device description 4F, JR4.0, 100cm
Published 2023-09-11
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx false
OTC false
Sterile true
Single use true Product Codes# Code, Name table Code Name DQO Catheter, Intravascular, Diagnostic
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class DQO Catheter, Intravascular, Diagnostic Cardiovascular 2
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 26950900932490 Package GS1 5 In Commercial Distribution 46950900932494 Package GS1 60 In Commercial Distribution 06950900932496 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized, EAN-13 table Source identifier GTIN-14 normalized EAN-13 26950900932490 26950900932490 46950900932494 46950900932494 06950900932496 06950900932496 6950900932496
GMDN Terms# Term, Definition table Term Definition Angiographic catheter, single-use A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
Regulatory Flags# DUNS number 420827639 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 06950900900693 INT,SlideCath ACJL605F1125 2023-09-11 06950900900709 INT,SlideCath ACJL606F1125 2023-09-11 06950900900716 INT,SlideCath ACJR304F1100 2023-09-11 06950900900723 INT,SlideCath ACJR307F1100 2023-09-11 06950900900730 INT,SlideCath ACJR355F1125 2023-09-11 06950900900747 INT,SlideCath ACJR356F1125 2023-09-11 06950900900754 INT,SlideCath ACJR405F1125 2023-09-11 06950900900761 INT,SlideCath ACJR406F1125 2023-09-11 06950900900778 INT,SlideCath ACJR455F1100 2023-09-11 06950900900785 INT,SlideCath ACJR456F1100 2023-09-11 06950900900792 INT,SlideCath ACJR456F1125 2023-09-11 06950900900808 INT,SlideCath ACJR457F1100 2023-09-11 06950900900815 INT,SlideCath ACJR505F1125 2023-09-11 06950900900822 INT,SlideCath ACJR506F1125 2023-09-11 06950900900839 INT,SlideCath ACJR605F1125 2023-09-11 06950900900846 INT,SlideCath ACJR606F1125 2023-09-11 06950900900853 INT,SlideCath ACTIG24F1100 2023-09-11 06950900900860 INT,SlideCath ACTIG25F1100 2023-09-11 06950900900877 INT,SlideCath ACTIG27F1100 2023-09-11 06950900900884 INT,SlideCath ACTIG34F1100 2023-09-11
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